Fungicidal agent

ABSTRACT

The invention relates to a novel fungicidal agent in the form of a salt associate having the structural formula shown. The agent can be used for treating diseases caused by fungi, and also for preventing fungal damage to various materials and agricultural products. The present fungicidal agent is an associate of 5-[3,5-dichloro-2-hydroxy benzylidene)amino]-4-hydroxy-1H-pyrimidine-2-on with 1,2,3,4,5-pentahydroxy-6-methylaminohexane and has the formula (I). 
                         
This fungicidal agent exhibits a broad range of activity and high solubility, which increases the effectiveness of the use thereof in the form of solutions. Compounds were obtained in a crystalline form, and the structure thereof was established by means of magnetic resonance spectra in dimethyl sulfoxide.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Continuation of U.S. patent application Ser. No. 15/321,601, filed Dec. 22, 2016, which is a U.S. National Stage of International Patent Application No. PCT/RU2014/000452, filed on Jun. 24, 2014, which published as WO 2015/199572 on Dec. 30, 2015, all of which are hereby incorporated by reference in their entirety.

TECHNICAL FIELD

The invention relates to fungicidal agents and can be used for treating diseases caused by fungi and prevention of spoilage of various materials and agricultural products by fungi.

BACKGROUND ART

A very serious problem in modern medicine, veterinary medicine and plant cultivation is treatment of fungal, bacterial and viral diseases, many of which respond to therapy very poorly. This is due to lack of efficiency of existing drugs and variability of bacteria, leading to the emergence of resistant forms (see Fidel P. L. Jr, Vazquez J. A., Sobel J. D. Candida glabrata: review of epidemiology, pathogenesis and clinical disease with comparison to C. albicans 1999, 1:80-96. White T. Antifungal drug resistance in Candida albicans ASM News 8:427-433.

The above is important for veterinary medicine and industry, because there is deterioration of products due to development and spread of microorganisms.

There is a number of drugs for treatment of fungal infections: nystatin, amphotericin B, fluconazole and terbinafine (RLS medications Encyclopedia—2009, RLS, 2009. Moscow, 928). Each of them has significant drawbacks. Fluconazole exhibits mainly fungistatic effect and practically does not possess fungicidal properties [Pharmaceutical microbiology. Ed. by W. B. Hugo and A. D. Rassel Blackwell Scientific Publications, Oxford, 1987, 511 p].

Fluconazole may also be used to prevent deterioration of plants and agricultural products by fungi. It is also known that fluconazole is used in archive-keeping for paper treatment.

The main drawback of Nystatin is the low activity against multicellular fungi.

Amphotericin B is an active antifungal preparation, but it is very toxic.

There is a fungicidal agent, which is notable for the fact that it is a salt of 2.4-dioxo-5-(2-hydroxy-3.5-dichlorobenzylidene)amino-1.3-pyrimidine:

or its dimer:

wherein X is selected from the series: Na⁺, K⁺, Li⁺, NH₄ ⁺, RU 2448960 C1.

This technical solution is taken as a prototype of the present invention.

The drug has a pronounced antifungal activity with wide spectrum of effect.

However, this compound is very poorly soluble in aqueous media and in fats. The maximum value of solubility of the known drug in water is 0.002%, and for fats it is no more than 0.001% (octanol, which is a common model of lipids). The low solubility of the fungicidal agent prototype is due to the fact that the substance has a large particle size: length—30 mkm and section—about 300 nm, which does not promote dissolution of the substance neither in an aqueous medium nor in fats. Solutions with such concentration of the active substance are not sufficiently effective. At the same time the task of improvement of efficiency of use of a fungicidal agent in the form of solutions for use in human and veterinary medicine in the form of injections and inhalations and for treatment of a variety of materials and agricultural products is extremely urgent.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a fungicidal agent with wide spectrum of effect that is a highly soluble, which increases the efficiency of its use in the form of solutions.

According to the invention, the task set is solved by the synthesis of a fungicidal agent which is a salt associate 5-[3,5-rhothane-2-hydroxybenzylidene)amino]-4-hydrox-1H-pyrimidine-2-on with 1.2.3.4.5-pentahydroxy-6-methylaminohexane.

The applicant has not found any technical solutions identical to the present invention, which enables to conclude that the invention conforms to the criterion “Novelty” (N).

All the salts specified in formula (I) have been isolated in crystalline form. FIGS. 1-3 shows their photomicrographs.

To prove the associates' structure in formula (I), their proton magnetic resonance spectra in dimethylsulfoxide were recorded. A significant shift of the azomethine proton signal downfield (from 9.5 to 10 ppm) was registered, indicating the formation of a strong hydrogen bond.

Length of 70% of the particles of the presented substance is less than 10 μm, which provides an important new property of the object (technical effect): Increase in solubility in water up to concentrations of 0.3-0.4%, and for oil solutions—up to 0.25-0.3% (more than a hundred-fold magnification), which can significantly increase the efficiency of use of the drug solutions.

In the applicant's opinion, these circumstances enable to conclude that the presented technical solution conforms to the criterion “Inventive Step” (“IS”).

BRIEF DESCRIPTION OF DRAWINGS

FIGS. 1-3 shows photomicrographs of the salts indicated in formula (I).

PREFERRED EMBODIMENT

A 0.1% solution of the presented agent was prepared as follows.

0.04 g of sodium hydroxide and 10 ml of 96% ethanol were placed into a flask. The mixture was heated until complete dissolution of sodium hydroxide. 0.127 g of 5-aminouracil was added portionwise to the resulting solution at 40° C. Then, the resulting mass was heated in a boiling water bath up to complete dissolution of aminouracil. Also, 0.191 g of 3.5-dichlorosalicyl aldehyde was dissolved in 40 ml of 96% ethanol. The resulting solution was dropwise added to a stirred solution of 5-aminouracil sodium salt. After the formation of an orange-red precipitate, the reaction mixture heating was continued for 1.5 hours; after cooling of the reaction mass to room temperature the precipitate was filtered off, washed with 10 ml of 96% ethanol and dried. The resulting precipitate was transferred to a flask containing a prepared solution of 0.195 1,2,3,4,5-pentahydroxy-6-methylaminohexane in 300 ml of water. The reaction mixture was stirred at t=40° C. until complete dissolution of the precipitate. The resulting solution was cooled to room temperature.

Preparation of a higher concentration solutions of the presented substance is similar.

For treatment of fungi in medical, veterinary and agricultural purposes aqueous or oil solutions of the preparation at a concentration of 0.1% were used.

To prevent deterioration of various materials by fungi, aqueous solutions at a concentration of 0.3% were used.

Except for water, suitable solvents and transporters include isotonic sodium chloride solution, Ringer's solution and the like, wherein for a stabilizer can be used benzyl alcohol or any material suitable for this purpose; to increase the bioavailability, fluorocarbons can be used for suction activator. To prepare an oil solution of the drug is necessary to use non-volatile oils that are commonly used to produce oily solutions or suspensions.

Any non-volatile neutral oil, including synthetic mono- or diglycerides, and fatty acids, is suitable for this purpose. To make injectable preparations, oleic acid and glycerides, olive or castor oil (especially in their polyoxyethylated derivatives) can be used. The composition of oil solutions or suspensions may also contain stabilizers and detergents in the form of long chain alcohols or other similar substances. If the drug formulation is prepared in the form of an aqueous suspension for inhalation or nasal sprays, emulsifiers and substances conferring to the drug a sweet taste, a pleasant odor and color can be added to the active agent.

EXAMPLE 1

Treatment of Respiratory Diseases.

The tests were conducted on white scrub mice (female, 6-8 weeks) received from “Rappolovo” breeding nursery (Leningrad reg.), which were kept under supervision for two weeks prior to the experiments on a standard diet in regulated vivarium conditions. Selection of the animals for the experiment group was conducted by the random selection method.

For propagation of aspergillus pneumonia, the white scrub mice received a single intraperitoneal injection of a cyclophosphamide solution (150 mg/kg). After 3 days, the mice received a single intraperitoneal injection of a hydrocortisone solution (250 mg/kg). Twenty-four hours after administration of hydrocortisone the mice were intranasally infected with a suspension of Aspergillus niger (approximately 10⁷ cells/ml) under ether narcosis.

On day 5 after infection 5 animals from each group were taken to study lung colonization (euthanasia in the rodents was performed by overdose of ether). Lung tissues were used to prepare homogenates, in which the titer of Aspergillus fungi was determined. Observation over the remaining mice was carried out for 14 days after infection to record their mortality.

The following groups of animals infected with Aspergillus niger were formed in the experiment.

1. Control groups: K1, K2, K3; the animals were exposed to an aerosol of isotonic sodium chloride solution.

2. Groups E1, E2, E3; the animals were administered a 0.1% aqueous solution of the presented preparation in the form of inhalations.

3. Groups P1, P2; the animals were administered an aqueous solution of the prototype fungicidal agent in the form of inhalations in concentrations of 0.002% and 0.001% respectively.

The animals were placed into an aerosol chamber (12 liters) for 30 minutes, during which period 500 mL of air pass through their lungs.

“OMRON U1” (Japan) ultrasonic nebulizer was used was used as an aerosol generator. To maintain a constant aerosol concentration in the chamber, a pneumatic vortex generator was used in the pulsed spraying mode ensuring a stable aerosol with particle size of 3 microns. The animals were placed in immobilization containers and exposed to the obtained aerosol for 30 minutes 1 time per day for 3 days starting from day 1 after the infection.

Samples of homogenized lung tissue were used to prepare a number of successive dilutions followed by sowing on Saburo medium. The results obtained are shown in Table 1.

The results shown in Table 1 confirm the effective antifungal activity of the presented fungicidal agent.

Results of the Study of the Fungicidal Agent's Antifungal Effect

TABLE 1 Groups of Number of colonies (in different dilutions) animals 10⁻² 10⁻⁴ 10⁻⁶ K1 75 2 — K2 64 2 — K3 48 — — E1 4 — — E2 4 — — E3 2 — — Π1 26 1 — Π2 37 2 —

EXAMPLE 2

Treatment of a Fungal Disease of the Skin—Scaly Skin Disease (Tinea Versicolor, Pityriasis versicolor).

The disease is caused by a fungus called Pityrosporum orbiculare-Malassezia furfur (mycelial form).

The following was prepared for the study: A 0.1% oil (olive oil) solution of the presented preparation and a 0.002% aqueous solution of the prototype substance. As a reference olive oil was used. The study included three groups of patients. Each group included 2 patients with this pathology. Treatment duration was 7 days. The drug was applied with a cotton swab 2 times a day—in the morning and in the evening.

As a criterion for mycological cure was considered the absence of yeast and mycelial forms of the Malassezia fungi, and the criterion of complete cure was the absence of clinical symptoms and fungi of the Malassezia genus in skin scales obtained from the skin at the areas of disappeared lesions.

The results of the study are shown in Table 2.

Results of Treatment of a Fungal Disease of the Skin—Scaly Skin Disease (Tinea Versicolor, Pityriasis versicolor)

TABLE 2 Preparation Mycological cure Complete cure 1 2 3 Reference Absent Absent 1 2 3 The presented yeast and mycelial forms Reached preparation of the Malassezia genus fungi are absent Prototype A slight decrease in yeast Absent and mycelial forms of the Malassezia genus fungi

Thus, a pronounced positive effect was achieved only when using the presented preparation.

EXAMPLE 3

Treatment of Vulvovaginal Candidiasis.

In the experiment, the patients, who suffered vulvovaginal candidiasis caused by Candida fungi, were treated using the following aqueous solutions: 1) 0.1% solution of the presented drug (3 persons), 2) 0.002% solution of the prototype drug (3 people).

The treatment in the form of dualfold (in the morning and in the evening) douchings was performed for 7 days. The treatment efficacy was assessed by the clinical presentation and the results mycological examination (inoculations on Saburo medium). The results of the study are shown in Table 3.

Results of Treatment of Vulvovaginal Candidiasis

TABLE 3 Preparation Mycological cure Complete cure Presented A tenfold reduction in the number Reached of fungi inoculated on a solid medium. Prototype 1.7-fold reduction in the number of Not reached fungi inoculated on a solid medium.

Thus, the use of the presented preparation allows to achieve a complete cure of Candida infection, whereas patients treated with an aqueous solution of the prototype substance showed a slight decrease of contamination by the fungus while maintaining the main complaints and manifestations of the infection.

EXAMPLE 4

Treatment of Fungal Diseases in Plants.

The study was conducted on tuberous begonias (Begonia tuberosa hybridum), infected with powdery mildew. Powdery mildew affects many plants, including trees and shrubs. Powdery mildew affects chrysanthemums, begonias, roses; at that a white, sometimes darkening, plaque appears green parts of the plant. The disease is transmitted by airborne spores.

The tested plants were infected with spores of a fungus (Leveillula taurica) when exposed up to appearance of a white plaque on the leaves. Three leaves on each plant were infected. After appearance of the plaque the plants in control group (three plants) were isolated from the three plants treated with a spray of a 0.1% aqueous solution of the presented preparation. The treatment was performed once a day for 7 days. After the treatment was complete, observation over the plants was continued for another three weeks. During the observation the control group plants showed an increase in the amount of plaque, which was a fungal mycelium, and the number of leaves infected increased on average up to 5-7, with plaque covering stems as well. The plants treated with the tested substance, no increase or spread of the fungus to other parts of the plant occur. When flushed off the leaf and inoculated on a nutrient medium, no growth of the fungi was observed.

EXAMPLE 5

Treatment of Fungal Diseases in Animals.

The preparation was used in treatment of ringworm in cats (two animals) caused by fungi of the Microsporum genus and characterized by appearance of small round bald patches on the face and ears of the animal. The preparation in the form of a 0.1% aqueous solution was applied onto the affected area three times a day for 6 days.

As a result of the treatment, the affected areas ceased to increase, disappearance of inflammatory manifestations was reported. Inoculations of the swabs from the affected area after the treatment did not lead to growth on nutrient media.

Thus, use of the presented formulation was effective for treatment of dermatomycosis caused by Microsporum fungus.

EXAMPLE 6

Protection of Construction Wood Against Fungal Attacks.

To test the preparation boards by the dimensions of 20×40×2 cm were used. The boards were divided into three groups. Group 1: the boards were impregnated with a 0.3% aqueous solution of the presented formulation. The impregnation was carried out by twofold application of the solution by means of a diffuser with an intermediate drying. Group 2: the boards were impregnated with a 0.02% aqueous solution of the prototype preparation. The impregnation was carried out by twofold application of the solution by means of a diffuser with an intermediate drying. Group 3 (control): the boards were impregnated with distilled water. The impregnation was carried out by twofold application of water by means of a diffuser with an intermediate drying.

The boards dried after treatment were soaked in water for two hours, after which they were coated with Aspergillus niger and Penicillium notatum fungi cultures at opposite ends of one side. The boards were placed in thermostats for 5 days at the temperature of 30° C. in a humid environment. After incubation, the boards were visually inspected and inoculations were made from their surface onto a nutrient medium (Sabouraud).

The result revealed that on the boards in the control group or those treated with a 0.02% aqueous solution of the prototype preparation a growth of the inoculated test bacteria can be detected, which later spread in the nutrient medium. No growth of the test organisms was registered on the boards impregnated with a 0.3% solution of the presented fungicidal agent, and the control inoculations did not lead to a growth on the nutrient medium.

INDUSTRIAL APPLICABILITY

The invention is implemented using common materials and equipment, resulting, according to the applicant's opinion, in compliance of the invention with the “Industrial Applicability” (“IA”) patentability criterion. 

The invention claimed is:
 1. A pharmaceutical dosage form comprising an effective amount of the compound of formula (I)

wherein X is selected from the group consisting of: Na⁺, K⁺ and NH₄ ⁺; and a dotted line is a hydrogen bond, and wherein said dosage form is suitable for administration by a nebulizer.
 2. The pharmaceutical dosage form of claim 1, wherein said dosage form is a solution for inhalation.
 3. The pharmaceutical dosage form of claim 2, wherein the solution is an aqueous solution.
 4. The pharmaceutical dosage form of claim 2, wherein the solution comprises about 0.1% of the compound of formula (I).
 5. The pharmaceutical dosage form of claim 1, wherein said dosage form is a suspension for inhalation.
 6. The pharmaceutical dosage form of claim 5, wherein the suspension is an aqueous suspension.
 7. The pharmaceutical dosage form of claim 5, wherein the suspension comprises about 0.1% of the compound of formula (I).
 8. The pharmaceutical dosage form of claim 1, wherein X is Na⁺.
 9. The pharmaceutical dosage form of claim 1, wherein X is K⁺.
 10. The pharmaceutical dosage form of claim 1, wherein X is NH₄ ⁺.
 11. A method of treating a respiratory disease in a subject in need thereof comprising administering to the subject an effective amount of the compound of formula (I)

wherein X is selected from the group consisting of: Na⁺, K⁺ and NH₄ ⁺; and a dotted line is a hydrogen bond, and wherein the compound of formula (I) is administered by a nebulizer.
 12. The method of claim 11, wherein the respiratory disease is pneumonia.
 13. The method of claim 11, wherein the respiratory disease is fungal pneumonia.
 14. The method of claim 11, wherein the respiratory disease is caused by Aspergillus fungus.
 15. The method of claim 11, wherein the compound is administered 1 time per day.
 16. The method of claim 11, wherein the compound is administered for at least 3 days.
 17. The method of claim 11, wherein the compound is in a form of a solution for inhalation.
 18. The method of claim 17, wherein the solution is an aqueous solution.
 19. The method of claim 17, wherein the solution comprises about 0.1% of the compound of formula (I).
 20. The method of claim 11, wherein the compound is in a form of a suspension for inhalation.
 21. The method of claim 20, wherein the suspension is an aqueous suspension.
 22. The method of claim 20, wherein the suspension comprises about 0.1% of the compound of formula (I).
 23. The method of claim 11, wherein X is Na⁺.
 24. The method of claim 11, wherein X is K⁺.
 25. The method of claim 11, wherein X is NH₄ ⁺.
 26. A nebulizer comprising an effective amount of the compound of formula (I)

wherein X is selected from the group consisting of: Na⁺, K⁺ and NH₄ ⁺; and a dotted line is a hydrogen bond. 